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Clinical Research Assistant
Velocity Clinical Cleveland, OH
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$56k-74k (estimate)
Full Time Just Posted
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Velocity Clinical is Hiring a Clinical Research Assistant Near Cleveland, OH

Overview

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Summary:

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.

Responsibilities

Duties/Responsibilities:

* Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity's SOPs

* Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations

* With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations

* Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable

* Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial

* Enter source data into the sponsor's and/or vendor's data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator

* Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team

* Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator

* Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects

* Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial

* Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person

* Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information

* Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team

* Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed

* Prepare source document charts, copy and/or file medical records and study related documents as required.

* Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.

* Other duties as assigned

Qualifications

Education/Experience:

* High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Required Licenses/Certifications:

* Phlebotomy if applicable and required by state law

* Intramuscular dose administration and preparation if applicable and required by state law

Required Skills:

* Demonstrated knowledge of medical terminology

* Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.

* Understanding of verbal, written, and organizational skills

* Demonstrated ability to work as a team player

* Demonstrated ability to read, write, and speak English

* Demonstrated ability to multi-task

* Demonstrated ability to follow written guidelines

* Demonstrated ability to be flexible/adapt as daily schedule may change rapidly

Required Physical Abilities:

* Sit or stand for long periods of time

* Communicate in person and by a telephone

* Limited walking required

* Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

Job Summary

JOB TYPE

Full Time

SALARY

$56k-74k (estimate)

POST DATE

04/30/2024

EXPIRATION DATE

05/13/2024

The following is the career advancement route for Clinical Research Assistant positions, which can be used as a reference in future career path planning. As a Clinical Research Assistant, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Assistant. You can explore the career advancement for a Clinical Research Assistant below and select your interested title to get hiring information.

Velocity Clinical Research
Full Time
$59k-78k (estimate)
6 Months Ago

If you are interested in becoming a Clinical Research Assistant, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Clinical Research Assistant for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Clinical Research Assistant job description and responsibilities

Certifications are also available for this position through The Society of Clinical Research Associates (SOCRA) and The Association of Clinical Research Professionals.

01/04/2022: Santa Barbara, CA

Analyze and evaluate clinical data gathered during research.

01/02/2022: Vincennes, IN

Provide regular report updates of the progress of clinical studies to the appropriate personnel.

03/23/2022: Santa Cruz, CA

These clinical trials are very much regulated and seriously monitored to ensure that they comply with the laid down regulations.

01/04/2022: Frankfort, KY

Must be able to ensure that data gotten from clinical trials are accurate and reliable and the legal rights and privacy of the subjects are protected.

02/02/2022: Racine, WI

Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Clinical Research Assistant jobs

Fact-checking, editing, and proofreading research documents for accuracy and consistency.

01/16/2022: Green Bay, WI

Research Assistants provide support to research teams who are conducting experiments or gathering and analysing data.

03/14/2022: Provo, UT

Maintained FDA clinical trial documentation for department and received excellent FDA audits of records.

03/02/2022: Fort Wayne, IN

Have strong customer focus and good communication skills

02/11/2022: Milwaukee, WI

For example, clinical research associate candidates should have excellent attention to detail and organizational skills since they’re responsible for monitoring and reporting on the results of clinical trials.

12/27/2021: Everett, WA

Step 3: View the best colleges and universities for Clinical Research Assistant.

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